Medical Device Manufacturer · ID , Bandung

N.V. Kalibaru - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1989

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - N.V. Kalibaru General Hospital ✕

1 devices

1-1 of 1

Cleared Jul 14, 1989

PATIENT EXAMINATION GLOVES (LATEX)

General Hospital · 102d